Neudle.com: temporal muscle

Differential
(Click to cross reference)

abdominal distention

abdominal protrusion

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acrocyanosis

acute disseminated encephalomyelitis

acute necrotizing encephalitis

acyl CoA dehydrogenase deficiency

addiction, heroin

Addison's disease

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alternating rapid movement, impaired

alveolar hypoventilation

amaurosis fugax

amaurosis fugax, unilateral vs.bilateral

ammonia

amnesia

AMPA receptor antibodies

amphiphysin antibodies

amyloid

amyloid angiopathy, cerebral

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, complications with

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

aneurysm, aortic arch

aneurysm, thoracic aortic

angiitis

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angina pectoris

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, cerebral, false negative

anterior horn cell disease

anti citrullinated antibody

antibiotics, neurologic complications with

antibodies to measles

anticonvulsants

anticonvulsants, blood level determination of

anticonvulsants, mechanism of action of

anticonvulsants, selection of

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

antineutrophil cytoplasmic autoantibodies

antiviral agents

aortic arch stenosis

aortic arch study

aortic wall, thickened

aortitis

aphasia

aphasia, progressive, primary

aphonia

apnea

apraxia

apraxia, constructional

arterial dissection, aorta

arterial dissection, wall thickness

autoimmune basal ganglia encephalitis

autoimmune cerebellar ataxia

autoimmune disease

autoimmune GFAP astrocytopathy

autonomic dysfunction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder, acute

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

Borrelia miyamotoi infection

brain biopsy, false negative

brain biopsy, negative

brain purpura

brainstem, atrophy

brainstem, dysfunction

brainstem, infarction of

brainstem, lesion of

Brown-Vialetto-Van Laere syndrome

bulbar palsy, progressive

calcification, lymph node

calf hypertrophy

camptocormia

cane

carbon monoxide poisoning

cardiac arrest and resuscitation

cardiac enzymes

cardiomyopathy

cardiovascular disease

caribbean

carnitine deficiency

carnitine deficiency myopathy

carotid artery disease

carotid artery stenosis

carpal tunnel syndrome

CAT scan

CAT scan, abnormal

CAT scan, angiography

CAT scan, chest

CAT scan, emission, abnormal

CAT scan, gray matter enhancement

CAT scan, muscle

cataracts

catatonia

cauda equina, enhancement

caudate nucleus, atrophy

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

cavernous sinus

cavernous sinus, expansion

cavernous sinus, lesion of

CD4 counts

ceftazidime

central hypoventilation

central nervous system, infection of

central pontine myelinolysis

cephalosporins

cerebellar ataxia, children

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar edema

cerebellar lesion

cerebellitis

cerebellum, disease of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral embolism

cerebral infarction, hemorrhagic

cerebral vasculature

cerebral venous thrombosis

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, cytology, false negative

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, IgG index, elevated

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, complications with

cerebrovascular accident, location of

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, postoperative

cerebrovascular accident, prognosis in

cerebrovascular accident, seizure with

cerebrovascular accident, topographic pattern

cerebrovascular disease

cerebrovascular disease, cardiovascular disease with

cerebrovascular disease, surgical treatment of

cerebrovascular disease, treatment of

cervical myelopathy

Charcot-Marie-Tooth

chemosis

chemotherapy, CNS treatment and complications with

cherry red spot-myoclonus syndrome

chromosomal abnormality

chromosome 19

chromosome 2

chromosome 5

chronic progressive external ophthalmoplegia

Churg-Strauss syndrome

cingulate gyrus

Clarkson disease

climate change

Clinical Pathologic Conference(C.P.C.)

clonus

clubfoot as related to neurologic disease

cognition

cogwheel rigidty

cold intolerance

collagen vascular disease

collapsin response mediator protein 5 IgG

confusional state, acute

congenital heart disease

congestive heart failure

conjunctivitis

consanguinity

constipation

contactin associated protein like 2 antibodies

contraction band necrosis

contractures, joint

controversies in neurology

conversion reaction

copper deficiency

corneal reflex, abnormal

corneal reflex, absent

coronary artery bypass

coronary artery disease

corpus callosum

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical deafness

cortical hemorrhage

cortical-basal ganglionic degeneration

cough

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

degenerative cervical myelopathy

degenerative diseases of CNS

delay in diagnosis

delayed muscle relaxation

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

dementia, transmissible

demyelinating disease

dental malocclusion

dental prostheses

dentatorubral-pallidoluysian atrophy

denture cream

depression

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

diamond on quadriceps

diarrhea

diarrhea, bloody

differential diagnosis

difficulty climbing stairs

diplopia

disability, neurological

disorientation

distal muscle atrophy

distal muscle weakness

dizziness

dopa responsive dystonia

downward deviation of eyes

doxycycline

DPPX, antibodies, encephalitis

Dravet syndrome

drooling

dropped head syndrome

drowsiness

drug abuse

drug abuse, neurologic complications of

drug induced neurologic disorders

dyskinesia, buccal lingual facial

dystrophic calcification

dystrophin

ears of the Lynx MR sign

electrocardiogram, abnormal

electrocorticogram

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electroencephalogram, video monitoring with

electromyogram

electromyogram, decremental response

electrophoretic pattern, serum

ELISA

embolism, atheromatous

embolism, cholesterol

embolism, platelet

emergencies, neurologic

emergency room

Emery-Dreifuss muscular dystrophy

emotional lability

encephalitis

encephalitis, acanthamoeba

encephalitis, amebic

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, etiology

encephalitis, focal

encephalitis, human immunodeficiency virus type 1

encephalitis, paraneoplastic

encephalitis, Powassan

encephalitis, Rasmussen's

encephalitis, viral

encephalomyelitis

encephalomyelitis, autoimmune

encephalomyelitis, paraneoplastic

encephalopathy

encephalopathy, anoxic

encephalopathy, delayed

encephalopathy, post anoxic

encephalopathy, progressive

endarterectomy, carotid

endarterectomy, carotid-complications of

endarterectomy, carotid-indications for

endarterectomy, carotid-long term results

endemic area

endocarditis, neurologic manifestations with

enteritis

enuresis

enzyme, defect

enzyme, muscle disease

enzyme, serum

eosinophilia

eosinophilic fasciitis

eosinophilic granulomatosis with polyangiitis

epidemiology of neurology

epilepsia partialis continua

episcleritis

episodic disorders

episodic neurologic deficits

episodic unconsciousness

erectile dysfunction

escherichia coli

euthanasia

executive dysfunction

exercise

exercise intolerance

exercise-induced neurologic dysfunction

exome sequencing

extralimbic encephalitis

extraocular muscle enlargement

extraocular muscle lesion

eye movement, disorders of

eye movement, painful

eye, pain in

face, numbness of

facial appearance, abnormal

facial pain

facial weakness

facial weakness, bilateral

faciobrachial dystonic seizure

failed medical management

fatal familial insomnia

fine motor function, impaired

finger nose finger test

fluorescein angiography

fourth ventricle, compression

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal behavioral spatial syndrome

frontal lobe, atrophy

frontotemporal dementia, behavioral variant

fundus, abnormality of

gamma amino butyric acid

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

ganglionitis

gastric partitioning

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastroparesis

gaze palsy

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

genetic diagnosis, prenatal

genetic neurologic disorders

glutamic acid decarboxylase, antibody

glycine

glycine receptor antibodies

glycogen storage disease

Gowers maneuver

granulomatosis with polyangiitis

granulomatous disease

grasp reflex

gray matter

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

gynecomastia

gyrus, abnormal

Hallervorden Spatz disease

hallucination

hallucination, visual

headache, chronic daily

headache, elderly

headache, etiology of

hearing loss, bilateral

hearing loss, sudden, bilateral

heart block

heart murmur

heel-knee-shin test

helminthic infection of CNS

hematuria, microscopic

hemianopia

hemiatrophy, cerebral

hemiplegia, progressive

hemispherectomy

hemolytic-uremic syndrome

hepatitis

hepatomegaly

heralding manifestation

herniated disc

herniated disc, cervical

herniation syndromes, intracranial

herpes simplex encephalitis

hiccoughs

high arched feet

high arched palate

highly active antiretroviral therapy

hippocampus, hyperintense

histochemistry of muscle

HLA

HMGcoA reductase inhibitors

hoarseness

homocysteine, serum

human immunodeficiency virus type 1

human T-lymphotropic virus type I(HTLV-I)

Huntington's chorea

Huntington's disease, children

hydrocephalus

hydrocephalus, exvacuo

hyperammonemic encephalopathy

hypercalcemia

hypercapnia

hyperekplexia

hypereosinophilic syndrome(HES)

hyperpigmentation of skin

hyperreflexia

hypersomnia

hypertension

hypertensive encephalopathy

hypertonia

hypertrophic intracranial pachymeningitis

hypertrophic spinal pachymeningitis

hypodontia

hypoglycemia

hypoglycorrhachia

hypokinetic left ventricle

hypotension, systemic

iatrogenic neurologic disorders

immune checkpoint inhibitors

immune-related adverse events

immunodeficiency

immunohistochemistry

immunologic disease

immunology and the nervous system

immunomodulation

immunosuppression

immunosuppressive agents

immunotherapy

impulsivity

inability to stand on tiptoes

inappropriate antidiuretic(A.D.H.)hormone

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inattention

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

incontinence, fecal

incoordination

infant, evaluation of

intellectual deterioration

intestinal pseudoobstruction

intracranial hypertension, benign

intracranial pressure, increased

intranasal medication

intrinsic hand muscles, wasting of

intubation

iron, brain

irritability

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, medical precaution with

Jakob-Creutzfeldt disease, variant

juvenile distal and segmental muscular atrophy

kelch-like protein 11 antibodies

ketogenic diet

lactate

lactic acidemia

lactic dehydrogenase(LDH)

Lafora body

Lafora's disease

laminectomy

laminectomy, cervical

learning disability, in children

leg atrophy

leg numbness

leg spasms, painful

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

leptospirosis

lethargy

leucine rich glioma inactivated 1 antibodies

leukemia

leukemia, neurologic findings assoc.with

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

level of consciousness, decreased

Lewy body

Lhermitte's sign

lid closure, weakness of

life expectancy

life support, withdrawal of

limb-girdle weakness

limbic encephalitis

linear lesion

lipid storage myopathy

liver function enzymes

lobar atrophy

locked-in syndrome

low back pain

lumbosacral plexopathy

lumbosacral radiculopathy

lymph node biopsy

lymphadenitis

lymphadenopathy

lymphadenopathy, hilar

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

Madonna facies

Maghreb

malabsorption

malabsorption syndrome

masseter muscle hypertrophy

masseter muscle tenomyositis

masseter muscle wasting

masseter muscle weakness

mediastinum, mass of

melanoma, malignant

MELAS syndrome

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal biopsy, false negative

meningeal enhancement

meningismus

meningitis

meningitis, basilar

meningitis, carcinomatous

meningitis, eosinophilic

meningitis, leptospira

meningitis, lymphomatous

meningitis, neutrophilic

meningitis, treatment of

meningoencephalitis

meningoencephalitis, amoebic

meningoencephalomyelitis

mental status, abnormal

mental status, abnormal, acute

methylmalonic acid, serum

methylmalonic acidemia

microaneurysm, retinal

microangiopathic hemolytic anemia

microangiopathy, brain

middle cerebellar peduncle, lesion

mitochondrial disease

mitochondrial encephalomyopathy

MNGIE syndrome

molecular genetics

monoclonal antibodies

monoclonal gammopathy

mononeuritis multiplex

mononeuropathy

mononeuropathy chronic inflammatory demyelinating

mononeuropathy multiplex

mononeuropathy, motor

motor neuron disease, misdiagnosis

motor symptoms

motor system

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, angiography, false negative

MRI, contrast enhanced

MRI, cortical enhancement

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, emergent

MRI, extraocular muscle enhancement

MRI, false negative

MRI, FLAIR

MRI, gray matter enhancement

MRI, lumbosacral plexus

MRI, muscle

MRI, negative

MRI, orbit

MRI, paramagnetic effect

MRI, pelvis

MRI, peripheral nerve

MRI, spinal cord

MRI, spine

MRI, sulcal hyperintensity

MRI, susceptibility weighted

MRI, vessel wall

MRI, vessel wall enhancement

MRS

multimodal neuroimaging

multinucleated giant cell

multiple organ failure

multiple sclerosis

muscle atrophy, progressive

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

muscular dystrophy, pattern of muscle involvement

mutism

myasthenia gravis

myasthenia gravis, paraneoplastic

myasthenia gravis, receptor site in

myasthenic syndrome

myelination of nervous system

myelinolysis, extrapontine

myelitis, longitudinal

myelitis, transverse, recurrent

myelomalacia

myeloneuropathy

myelopathy

myelopathy, chronic progressive

myeloradiculopathy

myocardial infarction

myoclonus, post anoxic

myoclonus, segmental

myoclonus, stimulus sensitive

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, genetic

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, inclusion body, hereditary

myopathy, metabolic

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, necrotizing

myopathy, necrotizing, autoimmune

myopathy, necrotizing, immune-mediated

necrotizing vasculitis

negative

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, intracranial

neoplasm, primary of CNS

neoplastic angioendotheliosis

nephritis

nerve biopsy

nerve conduction studies

nerve enlargement

nerve root biopsy

nerve root enhancement

nerve root hypertrophy

neurexin-3 alpha antibodies

neuritis, causes of

neuroaxonal leukodystrophy

neuroendocrinology

neurogenic bladder

neurogenic stunned myocardium

neuroleptic, atypical

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic disease, tempo

neurologic evaluation

neurologic examination, focal

neurologic signs

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromyelitis optica (Devic's disease)

neuromyelitis optica spectrum disorder

neuromyotonia

neuromyotonia and axonal neuropathy

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronopathy

neuronopathy, sensory

neuronopathy, sensory and motor

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, chronic

neuropathy, demyelinating

neuropathy, ischemic

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, toxic

neuropathy, vasculitic, systemic

next-generation sequencing

nonsteroidal anti-inflammatory drug

nonverbal

numbness, extremity

numbness, generalized

nusinersen

nutritional deficiency

nystagmus

nystagmus, monocular

nystagmus, primary position of gaze

nystagmus, rotary

ocular motility, disorders of

oculocephalic reflex

old age, neurology of

onconeural antibodies

ophthalmic artery

ophthalmoplegia

ophthalmoplegia, progressive external

opportunistic infection

opportunistic infection, CNS

opsoclonus

opsoclonus-myoclonus syndrome

optic atrophy

optic neuropathy

optic neuropathy, ischemic

optic neuropathy, ischemic, anterior

oral contraceptives

orbit, mass

ornithine transcarbamylase deficiency

osmotic demyelination syndrome

ovarian tumor

owl's eye sign of spinal cord

pachymeningitis, cranial

paralysis, acute areflexic

paralysis, asymmetric

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paraparesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraproteinemia

parasitic infection

parasitic infection, CNS

parasomnia

paraspinal muscle

paraspinal muscle weakness

paresthesias

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinson disease, dystonia with

Parkinson disease, etiology of

Parkinson disease, L-dopa nonresponsive

Parkinson disease, nonmotor problems of

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinsonism syndrome

Parkinsonism, freezing phenomena in

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

pathology

percussion induced muscle contraction

periarteritis nodosa

perineuritis

perineuritis, optic

peripheral nerve, lesion of

persistent vegetative state

pituitary stalk, lesion of

pituitary, lesion of

plasmacytoma

PLEDs

PLEDs, bilateral independent

pleocytosis of cerebrospinal fluid

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polymyalgia rheumatica

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyuria

pons, infarction of

pons, lesion of

pontocerebellar atrophy

positive sharp waves

posterior column disease

posterior leukoencephalopathy syndrome

potassium channel antibodies

practice guidelines

precipitating factors

pregnancy, neurologic complications in

pressure sores

primary lateral sclerosis

prion disease

prognosis

progressive encephalomyelitis with rigidity syndrome

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive supranuclear palsy

prolactin, elevated

propofol

proprioception, abnormal

protein 14-3-3, cerebrospinal fluid

proteinuria

protozoan infection

proximal muscle atrophy

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pulmonary function tests

pulmonary infiltrates

pulvinar sign

pupil, dilated and fixed, bilateral

purpura

pursuit eye movements, abnormal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quadriparesis, acute

quadriparesis, progressive

quadriplegia

quality of life

rabies, nervous system involvement with

raccoon

radiation therapy, CNS treatment and complications with

radiculopathy

ragged-red fibers

Rankin score

rapid onset dystonia parkinsonism

rapidly fatal neurologic illness

rapidly progressing neurologic illness

rash

rash, hand

Raynaud's phenomenon

real-time quaking-induced conversion

recurrent

Red flags

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal failure

renal tubular acidosis

repetitive nerve stimulation

respirations in CNS disease

respirator

respiratory distress syndrome, neurologic status with

respiratory failure

respiratory tract infection

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

retinal lesion

retinal microvascular disease

rheumatoid arthritis factor(R.A.factor)

rheumatoid arthritis, neurologic complications of

rheumatoid vasculitis

rhinorrhea

rhomboencephalopathy

riboflavin

riboflavin transporter deficiency

Rocky Mountain spotted fever

saccadic eye movements, abnormal

safety

salivation, excessive

scleroderma, neurologic involvement with

sclerosis, bone

SCN1A gene

scoliosis

scoliosis, neurologic association with

sedimentation rate, elevated

seizure

seizure, children

seizure, drug resistance

seizure, drug-induced

seizure, intractable, treatment of

seizure, surgical treatment of

seizure, teenager

seizure, tonic-clonic

seizure, treatment of

sella trucica

seminoma

sensorineural hearing loss

sensory loss

sensory loss, asymmetric

sensory loss, patchy

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

serum alanine aminotransferase

sexual behavior, disorder of

skin, lesions in neurologic disorders

sleep apnea, obstructive

sleep pathology and physiology

slit lamp examination

slow virus infection of CNS

small vessel disease

SMN1 gene

snout reflex

sodium channel dysfunction

sodium valproate

sodium valproate, toxicity

somatosensory evoked potentials

somnolence

sonophobia

spastic ataxia

spastic paraplegia, type 11

spastic paraplegia, type 7

spasticity

speech disorder

speech disorder, childhood

speech, delayed development of

speech, loss of

speech, unintelligible

spinal cord, cervical

spinal cord, compression of

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, classification

spinal pachymeningitis

spinal stenosis

spinal stenosis, cervical canal

spinocerebellar ataxia

spinocerebellar ataxia type 2

spinocerebellar ataxia type 7

spirochete infection

spongy degeneration of brain

square wave jerks

standing difficulty

staphylococcal protein A column therapy

status epilepticus, intractable

status epilepticus, myoclonic

status epilepticus, nonconvulsive

stem cell transplantation

steppage gait

steroid

steroid therapy, CNS treatment and complications with

stiff legs

stiff man syndrome

stimulation, deep brain

stooped posture

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

stroke, progression of

strokelike episodes

stuporous

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subacute sclerosing panencephalitis, adult onset

sudden death

suicide

superior cerebellar peduncle

Susac's syndrome

sweating

symmetric brain lesions

synovitis

synucleinopathy

systemic illness

systemic lupus erythematosus

teeth, number of in infants

temporal artery

temporal artery, biopsy

temporal artery, tender

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle enhancement

temporalis muscle hypertrophy

temporalis muscle swelling

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint

temporomandibular joint, dislocation

temporomandibular joint, pain

temporomandibular joint, synovitis

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thrombotic microangiopathy

thrombotic thrombocytopenia purpura

tick-borne encephalitis

titubation

toe walking

tone, muscle

tone, muscle, increased

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, weakness

tonic foot response

tonic spasms

tonsillar herniation of cerebellum

transient ischemic attack

transient neurologic deficit

transluminal angioplasty, coronary artery

transverse smile

trauma

travel, foreign

treatment of neurologic disorder

trigeminal nerve, abnormality of

trigeminal neuralgia

trigeminal neuropathy

trigeminal neuropathy, motor

trinucleotide repeats

tripping

typhus, scrub

tyrosine hydroxylase deficiency

unconsciousness, episodic

unconsciousness, transient

undiagnosed

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

vascular endothelial growth factor

vasculitides

vasculitis, large vessel

vasculopathy

ventricular enlargement

vertebral artery wall thickness

vertigo

vibratory sensation, abnormal

vision, blurred, monocular

visual acuity, decreased

visual acuity, decreased, monocular

visual field defect

visual impairment

visual loss

visual loss, alternating

visual loss, sudden-unilateral

visual loss, transient

visual symptoms

visuospatial disturbance

walking, difficulty with

weakness, fluctuating

weakness, focal

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

weight loss

Werdnig-Hoffman disease

white matter disease, subcortical

wide based gait

winging of scapula

word-finding difficulty

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Neurol 92:e274-e281, Chen, Z. & Neo, S., 2019

Clinicopathologic Conference, Powassan Virus Encephalitis
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Muscular Dystrophies
Lancet 394:2025-2038, Mercuri, E.,et al, 2019

Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
Neurol 93:939-944, Torabi,T.,et al, 2019

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Pantothenate Kinase - Associated Neurodegeneration (PKAN)
Emedicine.Medscape Sept, Hanna, P.A. & Benbadis, S.R., 2018

Progressive Gait Difficulty and Incontinence in a 40-year-old Man with HIV
Neurol 91:1065-1070, Silverman, A.,et al, 2018

Clinical Reasoning: A 49-year-old man with Progressive Numbness, Weakness, and Evidence of Leptomeningeal Enhancement
Neurol 90:e90-e93, Lovett, A.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

Degenerative Cervical Myelopathy
BMJ 360:k186, Davies, B.M.,et al, 2018

Subacute Paresis in a 28-year-old man with HIV
Neurol 90:432-435, Harada, Y.,et al, 2018

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

A young woman with symmetric weakness and behavioral disturbance
Neurol 90:e1442-e1447, Rosenberg, J.,et al, 2018

A 42-year-old man with unilateral leg weakness
Neurol 90:e1085-e1090, Schneider, R.,et al, 2018

A 75-year-old man with parkinsonism, mood depression, and weight loss
Neurol 90:572-575, Frattini, E.,et al, 2018

Persistent Respiratory Failure Following Cardiac Arrest
Neurol 90:e2174-e2178, Fullam, T. & Sladky, J.H., 2018

A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
Neurol 91:187-190, Silva,A.M.S.,et al, 2018

A 58-year-old Woman with Systemic Scleroderma and Progressive Cervical Cord Compression
Neurol 91:e1262-e1264, Karschnia, P.,et al, 2018

Neuromyelitis Optica Spectrum Disorder (NMOSD) in a Male with Hiccups and Quadriparesis
IJCMR 5:K28-K30, Tuteja,H.S.,et al, 2018

Making Sense of the Clinical Spectrum of Limb Girdle Muscular Dystrophies
Pract Neurol 18:201-210, Khadilkar,S.V.,et al, 2018

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Clinicopathologic Conference, Copper Deficiency Myelopathy
NEJM 377:1977-1984, Case 35-2017, 2017

An 82-year-old man with Worsening Gait
Neurol 89:e246-e252, Chew, S.,et al, 2017

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017

A 58-year-old man with Progressive Ptosis and Walking Difficulty
Neurol 89:e1-e5, Kuo, P.,et al, 2017

Neuroimaging Changes in Menkes Disease, Part 1
AJNR 38:1850-1857, Manara, R.,et al, 2017

A 55-year-old Man with Rapidly Progressive Dementia and Parkinsonism
Neurol 89:e182-e187, Tabuas-Pereira, M.,et al, 2017

A 15-month-old boy with Progressive Lethargy and Spasticity
Neurol 89:e135-e139, Zhang, R.,et al, 2017

Clinicopathologic Conference, Eosinophilic Granulomatosis with Polyangiitis
NEJM 377:1569-1578, Case 32-2017, 2017

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
NEJM 377:1713-1722,1786, Mendell, J.R.,et al, 2017

Nusinersen Versus Sham Control in Infantile-Onset Spinal Muscular Atrophy
NEJM 377:1723-1732,1786, Finkel, R.S.,et al, 2017

Clinical Pathologic Conference, West Nile Virus Encephalitis
NEJM 377:1878-1886, Case 34-2017, 2017

A Case of Statin-Associated Autoimmune Myopathy
Clin Med Insights: Case Reports 10:1-4, Sweidan, A.J.,et al, 2017

Clinicopathologic Conference, Granulomatous Amebic Encephalitis and Sarcoidosis (Inactive)
NEJM 376:368-379, Case 3-2017, 2017

Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
JAMA Neurol 74:238-241, Dubey, D.,et al, 2017

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

Precipitous Deterioration of Motor Function, Cognition, and Behavior
JAMA Neurol 74:591-596, Fernandez-Fournier, M.,et al, 2017

A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
Neurol 88:e185-e189, Vazquez do Campo, R.,et al, 2017

Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
JAMA Neurol 74:737-740, Cohen, A.L.,et al, 2017

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017

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